Re-inventing Drug Development | Agenda Bookshop Skip to content
Online orders placed from 19/12 onward will not arrive in time for Christmas.
Online orders placed from 19/12 onward will not arrive in time for Christmas.
Age Group_Uncategorized
Age Group_Uncategorized
automatic-update
B01=Jeffrey S. Handen
Category1=Non-Fiction
Category=KC
Category=KJVN
Category=MBP
Category=MMG
Category=PN
Category=PSA
Category=TDCW
COP=United States
Delivery_Pre-order
Language_English
PA=Temporarily unavailable
Price_€100 and above
PS=Active
softlaunch

Re-inventing Drug Development

English

The biopharmaceutical industry has entered an era of unprecedented change and challenge, characterized by increasing pricing pressures, rising rates of attrition in the product development lifecycle, and decreasing scientific innovation. The most successful products are losing patent protection, and pipelines have been unable to fill the gap. This book explores the evolving definition of innovation in therapeutic product development and begins to examine its effects on the life sciences R&D industry.

Historically, scientific innovation alone was sufficient to maintain ROI and deliver on unmet medical needs. However, with many forces now conspiring to increase pressures on the commoditization of drug development, industry support for truly novel, often high-risk development has eroded. This calls for a drastic redefinition of what innovation is. While innovation in the pharmaceutical R&D industry has historically been applied to major advances in therapy and unmet medical needs, we now need to see innovation increasingly defined in terms of financial, marketing (e.g. branded generics and emerging markets), pharmacoeconomic, and operational innovation.

In this book, contributors drawn from the executive ranks of clinical development practitioners and stakeholdersfrom biopharmaceutical companies, clinical research organizations, academia, the financial community, and the patient perspectivehave all come together to provide their expertise and visions. Their goal is to start a dialogue about ways to radically improve therapeutics development and get more and better medicines to the patients who need them, as fast as possible, in the most cost-efficient manner.

See more
Current price €170.09
Original price €188.99
Save 10%
Age Group_Uncategorizedautomatic-updateB01=Jeffrey S. HandenCategory1=Non-FictionCategory=KCCategory=KJVNCategory=MBPCategory=MMGCategory=PNCategory=PSACategory=TDCWCOP=United StatesDelivery_Pre-orderLanguage_EnglishPA=Temporarily unavailablePrice_€100 and abovePS=Activesoftlaunch

Will deliver when available.

Product Details
  • Weight: 440g
  • Dimensions: 156 x 234mm
  • Publication Date: 28 Oct 2014
  • Publisher: Taylor & Francis Inc
  • Publication City/Country: United States
  • Language: English
  • ISBN13: 9781466579989

About

Jeffrey S. Handen PhD is vice president of professional services with Medidata Solutions Inc. Dr. Handen has published in multiple peer-reviewed and business journals presented at numerous industry conferences and scientific meetings as an invited speaker and served as past editor-in-chief of the Industrialization of Drug Discovery compendium. Before joining Medidata Solutions he was with Merck Research Laboratories for 6 years as a director of portfolio and project management helping to plan manage and execute Mercks clinical development portfolio. Prior to Merck Dr. Handen held management consulting positions with Computer Science Corporation and IBM Business Consulting Services (formerly PricewaterhouseCoopers Consulting). With over 20 years of experience in pharmaceutical and biotechnology research and development process reengineering and systems and process implementation Dr. Handen has also held research and management positions with the University of Pennsylvania and the National Institutes of Health. As vice president of professional services for Medidata Solutions Dr. Handen is responsible for overseeing clinical development business process integration solution architecting for optimizing clinical trials design execution and development implementation of data-driven metrics and developing and implementing operational metrics to improve clinical research processes. He holds a PhD in neurosciences from George Washington University as well as a BS from Duke University.

Customer Reviews

Be the first to write a review
0%
(0)
0%
(0)
0%
(0)
0%
(0)
0%
(0)
We use cookies to ensure that we give you the best experience on our website. If you continue we'll assume that you are understand this. Learn more
Accept